More product quality issues at Sun

[anonymous]

They manufacture a drug for a European pharma company who has had to pull the product from the US market.

Again.

Sun has serious ongoing quality issues and their alleged world-class manufacturing site, Halol has been shut down multiple times by FDA.

Would you ingest a Sun Rx?

These are simple, verifiable facts.

 

[anonymous]

They manufacture a drug for a European pharma company who has had to pull the product from the US market.

Again.

Sun has serious ongoing quality issues and their alleged world-class manufacturing site, Halol has been shut down multiple times by FDA.

Would you ingest a Sun Rx?

These are simple, verifiable facts.

Yep. For years thereve been product shortages, product recalls, supply issues due to failure to meet quality specifications and so on.
But in the pursuit of a rupee, Sun continues and just sees these issues as a small bump.

When was a major US pharma company manufacturing site shut down by FDA?

 

[anonymous]

whats the product?

 

[anonymous]

https://amp.miamiherald.com/news/recalls/article277665608.html

Recall of ADHD med due to presence of metal.

OP learn how to post a source.

idiot that replied, learn how to use Google.

 

[anonymous]

https://amp.miamiherald.com/news/recalls/article277665608.html

Recall of ADHD med due to presence of metal.

OP learn how to post a source.

idiot that replied, learn how to use Google.

Hey asshole, OP here.
I purposefully didn’t post the link, and btw, it’s NOT for ADHD.

It’s another product

 

[anonymous]

Recent Sun Recalls

1. Sun Pharma UK Ltd has informed the MHRA of a labelling issue with one batch of Gemcitabine 2000mg/200ml infusion. (https://www.gov.uk/drug-device-aler...ion-bag-2000mg-slash-200ml-clmr-23-a-slash-06)
   
2. Health Canada announces that Sun Pharma Canada Inc. is recalling 2 lots of Cequa Ophthalmic Solution (cyclosporine 0.09% w/v) (lot number: 10026, 10027) from wholesalers, retailers and distributor because the stability assay is out of specification in the affected lots. (https://www.drugoffice.gov.hk/eps/n...ecification/consumer/2023-09-07/en/50972.html)
   
3. Drug Recall Enforcement Report Class III voluntary initiated by SUN PHARMACEUTICAL INDUSTRIES INC, originally initiated on 07-18-2023 for the product Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T of D & NH), India, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512. (https://ndclist.com/recalls/92725)
   
4. Princeton (New Jersey) based Sun Pharmaceutical Inc is recalling 16,450 vials of Norepinephrine Bitartrate Injection for "Failed Impurities/Degradation Specifications", it said (https://www.bqprime.com/amp/business/biz-drug-recall)
   
5. In a recent FDA enforcement report, the agency said the firm is pulling more than 34,000 bottles of generic diltiazem hydrochloride because the drug batch failed "stability testing and failed dissolution testing” at an FDA laboratory. (https://www.fiercepharma.com/manufa...ics-bottles-yanked-due-failed-testing-fda-lab)
   
6. Sun Pharmaceutical Industries is recalling 24,194 pre-filled syringes of Fyremadel (ganirelix acetate) injection, a drug used to treat infertility in women, in the US market due to a manufacturing issue, according to USFDA (https://www.expresspharma.in/amp/su...prefilled-syringes-of-infertility-drug-in-us/)